A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938615



Internal ID26474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116485612..116499474hg38UCSC Ensembl
chr3:116204459..116218321hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3813863
hg1913863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938615
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002811


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